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145241-93-6

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145241-93-6 Usage

Molecular weight

155.19 g/mol

Chemical class

Amines and polyamines

Main properties

Ester derivative of 2-azabicyclo[3.1.0]hexane-1-carboxylic acid, used in pharmaceutical research and drug development, potential applications in organic synthesis and medicinal chemistry

Specific content

Building block for synthesis of biologically active compounds

Check Digit Verification of cas no

The CAS Registry Mumber 145241-93-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,2,4 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 145241-93:
(8*1)+(7*4)+(6*5)+(5*2)+(4*4)+(3*1)+(2*9)+(1*3)=116
116 % 10 = 6
So 145241-93-6 is a valid CAS Registry Number.

145241-93-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (-)-(2S,3R)-2,3-methanoproline methyl ester

1.2 Other means of identification

Product number -
Other names (1S,5R)-2-aza-bicyclo[3.1.0]hexane-1-carboxylic acid methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:145241-93-6 SDS

145241-93-6Relevant articles and documents

First asymmetric synthesis of (-)-(2S,3R)-methanoproline

Hercouet,Bessieres,Le Corre

, p. 1267 - 1268 (2007/10/03)

The title amino acid was synthesized in enantiomerically pure form, starting from (S)-(-)-butanetriol 1, by condensation of cyclic sulfate 3 with methyl benzylideneglycinate.

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